Allele Registry

Canonical Allele Identifier: PA112890

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015476

ClinVar Variation:

14397

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Ala373Val	CA123926 NM_000233.4:c.1118C>T